Works matching IS 10597700 AND DT 2019 AND VI 28 AND IP 2

Results: 32

INTRODUCTION TO EXPLORING THE EXOME SPECIAL ISSUE.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 181, doi. 10.1002/jgc4.1113

By:

Resta, Robert G.;
Sullivan, Jennifer;
McConkie‐Rosell, Allyn

Publication type:

Article

Genetics professionals' attitudes toward prenatal exome sequencing.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 229, doi. 10.1002/jgc4.1112

By:

Brew, Casey E.;
Castro, Brian A.;
Pan, Vivian;
Hart, Alexa;
Blumberg, Bruce;
Wicklund, Catherine

Publication type:

Article

Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 456, doi. 10.1002/jgc4.1123

By:

Rashkin, Misha D.;
Bowes, Johnathan;
Dunaway, Keith;
Dhaliwal, Jasmine;
Loomis, Erick;
Riffle, Stephen;
Washington, Nicole L.;
Ziegler, Chris;
Lu, James;
Levin, Elissa

Publication type:

Article

Rapid clinical exome sequencing in a pediatric ICU: Genetic counselor impacts and challenges.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 283, doi. 10.1002/jgc4.1116

By:

Clowes Candadai, Sarah V.;
Bennett, James T.;
Sikes, Megan C.;
Thies, Jenny M.;
Freed, Amanda S.

Publication type:

Article

Understanding the present and preparing for the future: Exploring the needs of diagnostic and elective genomic medicine patients.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 438, doi. 10.1002/jgc4.1114

By:

East, Kelly M.;
Cochran, Meagan;
Kelley, Whitley V.;
Greve, Veronica;
Emmerson, Kristina;
Cochran, Jesse Nicholas;
Hott, Adam M.;
Bick, David;
Raines, Grace

Publication type:

Article

New developmental syndromes: Understanding the family experience.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 202, doi. 10.1002/jgc4.1121

By:

Adam, Shelin;
Christèle du Souich;
Mwenifumbo, Jill;
Nelson, Tanya N.;
van Karnebeek, Clara;
Friedman, Jan M.;
Inglese, Cara N.;
Elliott, Alison M.;
Lehman, Anna

Publication type:

Article

A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 213, doi. 10.1002/jgc4.1119

By:

Merker, Jason;
Schelley, Susan;
Enns, Gregory;
Montgomery, Stephen;
Zappala, Zach;
Fresard, Laure;
Prybol, Cameron;
Taylor, Robert;
McFarland, Robert;
Holmes, Matthew;
Thompson, Kyle;
Olahova, Monika;
Adams, David R.;
Aday, Aaron;
Alejandro, Mercedes E.;
Allard, Patrick;
Azamian, Mahshid S.;
Bacino, Carlos A.;
Baker, Eva;
Balasubramanyam, Ashok

Publication type:

Article

Genetic counseling for consumer‐driven whole exome and whole genome sequencing: A commentary on early experiences.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 449, doi. 10.1002/jgc4.1109

By:

Schmidt, Johanna L.;
Maas, Roxanne;
Altmeyer, Sharon Reid

Publication type:

Article

A novel approach to offering additional genomic findings—A protocol to test a two‐step approach in the healthcare system.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 388, doi. 10.1002/jgc4.1102

By:

Wale, Janney;
Martyn, Melissa;
Kanga‐Parabia, Anaita;
Gaff, Clara L.;
Lynch, Elly;
Keogh, Louise;
Halliday, Jane;
Goranitis, Ilias;
Downie, Lilian;
Brown, Natasha J.;
Amor, David;
Macciocca, Ivan;
Jarmolowicz, Anna;
Lunke, Sebastian;
Cunningham, Fiona;
James, Paul A.;
Trainer, Alison H.;
Walsh, Maie;
Winship, Ingrid;
Bogwitz, Michael

Publication type:

Article

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 367, doi. 10.1002/jgc4.1101

By:

Nisselle, Amy;
Vuong, Hannah;
McClaren, Belinda;
Metcalfe, Sylvia;
Gaff, Clara;
Dunlop, Kate;
Macciocca, Ivan;
McKenzie, Fiona

Publication type:

Article

Perspectives on facilitating whole exome sequencing for international patients at Mayo Clinic.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 398, doi. 10.1002/jgc4.1100

By:

Agre, Katherine;
Ewing, Sarah;
Gunderson, Lauren;
Kemppainen, Jennifer;
Murphree, Marine;
Bertsch, Nicole

Publication type:

Article

Secondary findings: How did we get here, and where are we going?

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 326, doi. 10.1002/jgc4.1098

By:

Ormond, Kelly E.;
O'Daniel, Julianne M.;
Kalia, Sarah S.

Publication type:

Article

Factors complicating the informed consent process for whole exome sequencing in neonatal and pediatic intensive care units.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 256, doi. 10.1002/jgc4.1097

By:

Diamonstein, Callie J.

Publication type:

Article

Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 428, doi. 10.1002/jgc4.1096

By:

Dagan‐Rosenfeld, Orit;
Bivona, Stephanie A.;
Snyder, Michael P.;
Rego, Shannon;
Ormond, Kelly E.

Publication type:

Article

Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 466, doi. 10.1002/jgc4.1094

By:

Adams, David R.;
Aday, Aaron;
Alejandro, Mercedes E.;
Allard, Patrick;
Ashley, Euan A.;
Azamian, Mahshid S.;
Bacino, Carlos A.;
Baker, Eva;
Balasubramanyam, Ashok;
Barseghyan, Hayk;
Batzli, Gabriel F.;
Beggs, Alan H.;
Behnam, Babak;
Bellen, Hugo J.;
Bican, Anna;
Bick, David P.;
Birch, Camille L.;
Boone, Braden E.;
Bostwick, Bret L.;
Briere, Lauren C.

Publication type:

Article

Using the diffusion of innovations model to guide participant engagement in the genomics era.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 419, doi. 10.1002/jgc4.1090

By:

Lewis, Katie L.;
Facio, Flavia M.;
Berrios, Courtney D.

Publication type:

Article

Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 304, doi. 10.1002/jgc4.1093

By:

Li, Xin;
Nusbaum, Rachel;
Dixon, Shannan;
Smith‐Hicks, Constance;
Mahida, Sonal;
Jamal, Leila

Publication type:

Article

Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 194, doi. 10.1002/jgc4.1091

By:

Macnamara, Ellen F.;
Schoch, Kelly;
McConkie‐Rosell, Allyn;
Kelley, Emily G.;
LeBlanc, Kimberly;
Fieg, Elizabeth;
Brokamp, Elly;
Signer, Rebecca;
Palmer, Christina G.S.

Publication type:

Article

Genetic counseling in pediatric acute care: Reflections on ultra‐rapid genomic diagnoses in neonates.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 273, doi. 10.1002/jgc4.1086

By:

Ayres, Samantha;
Brett, Gemma R.;
Gallacher, Lyndon;
Stark, Zornitza

Publication type:

Article

Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 292, doi. 10.1002/jgc4.1076

By:

Park, Jessica;
Zayhowski, Kimberly;
Ormond, Kelly E.;
Newson, Ainsley J.

Publication type:

Article

Patients' perspectives of variants of uncertain significance and strategies for uncertainty management.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 313, doi. 10.1002/jgc4.1075

By:

Makhnoon, Sukh;
Shirts, Brian H.;
Bowen, Deborah J.

Publication type:

Article

Genetic counseling considerations with rapid genome‐wide sequencing in a neonatal intensive care unit.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 263, doi. 10.1002/jgc4.1074

By:

Smith, Emma E.;
du Souich, Christèle;
Elliott, Alison M.;
Dragojlovic, Nick

Publication type:

Article

Indigenous Peoples and genomics: Starting a conversation.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 407, doi. 10.1002/jgc4.1073

By:

Morgan, Jenny;
Lesueur, Rochelle;
Kenny, Ruth;
Price, Roberta;
Coe, Rachel R.;
Makela, Nancy;
Birch, Patricia H.

Publication type:

Article

User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 240, doi. 10.1007/s10897-018-0298-5

By:

Roscioli, Tony;
Josephi‐Taylor, Sarah;
Kirk, Edwin P.;
Barlow‐Stewart, Kristine;
Selvanathan, Arthavan;
Worgan, Lisa;
Rajagopalan, Sulekha;
Colley, Alison;
Bittles, Alan;
Meiser, Bettina

Publication type:

Article

Interpretations of the Term "Actionable" when Discussing Genetic Test Results: What you Mean Is Not What I Heard.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 334, doi. 10.1007/s10897-018-0289-6

By:

Ryan, Kerry A.;
Gornick, Michele C.;
Uhlmann, Wendy R.;
Scott Roberts, J.;
De Vries, Raymond G.;
Scherer, Aaron M.

Publication type:

Article

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 343, doi. 10.1007/s10897-018-0288-7

By:

Vornanen, M.;
Aktan‐Collan, K.;
Haukkala, A.;
Hallowell, N.;
Konttinen, H.

Publication type:

Article

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 477, doi. 10.1007/s10897-018-0286-9

By:

Li, Meng;
Veenstra, David L.;
Bennette, Caroline S.;
Amendola, Laura M.;
Ragan Hart, M.;
Jarvik, Gail P.;
Heagerty, Patrick;
Comstock, Bryan;
Tarczy‐Hornoch, Peter;
Fullerton, Stephanie M.;
Burke, Wylie;
Trinidad, Susan B.;
Regier, Dean A.;
Patrick, Donald L.

Publication type:

Article

Comparison of medical management and genetic counseling options pre‐ and post‐whole exome sequencing for patients with positive and negative results.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 182, doi. 10.1002/jgc4.1054

By:

Neilson, Derek;
Zhang, Xue;
Valencia, C. Alexander;
Wusik, Katie;
Collins, Kathleen;
Matias, Margret

Publication type:

Article

Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 378, doi. 10.1002/jgc4.1053

By:

Dwarte, Tanya;
Barlow‐Stewart, Kristine;
O'Shea, Rosie;
Dinger, Marcel E.;
Terrill, Bronwyn

Publication type:

Article

Whole exome sequencing for prenatal diagnosis in cases with fetal anomalies: Criteria to improve diagnostic yield.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 251, doi. 10.1002/jgc4.1045

By:

Yadava, Stacy M.;
Ashkinadze, Elena

Publication type:

Article

Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results.

Published in:

Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 355, doi. 10.1002/jgc4.1048

By:

Seiffert, David J.;
McCarthy Veach, Patricia;
LeRoy, Bonnie;
Zierhut, Heather;
Guan, Weihua

Publication type:

Article

Issue Information.

Published in:: Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 177, doi. 10.1002/jgc4.1001
Publication type:: Article